Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content 		14 0 8 0.16 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 12 0.15 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 7 0.14 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 7 0.14 0 0
CUI: C4025571
Disease: Type 1 fibers relatively smaller than type 2 fibers
Type 1 fibers relatively smaller than type 2 fibers 		6 0 6 0.14 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 11 0.13 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 8 0.12 0 0
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 6 0.12 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 5 10 0.12 1 5.3E-02
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 14 0.12 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 7 0.12 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 6 0.12 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 6 0.12 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 9 0.12 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 4 9 0.12 1 5.6E-02
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 11 0.11 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 9 0.11 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 6 0.11 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 6 0.11 0 0
CUI: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 6 0.11 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 5 0.11 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		18 0 6 0.11 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 7 0.11 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 8 0.11 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy 		9 0 5 0.10 0 0